Canonical Allele Identifier: CA2584993504
Gene: IFNL3 HGNC NCBI

Linked Data

gnomAD v4: 19-39243628-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39243628A>G , CM000681.2:g.39243628A>G GRCh38
NC_000019.9:g.39734268A>G , CM000681.1:g.39734268A>G GRCh37
NC_000019.8:g.44426108A>G NCBI36
NG_042193.1:g.6344T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000613087.5:c.*4T>C ENSP00000481633.1:n.*4T>C
ENST00000413851.3:c.*4T>C MANE Select ENSP00000409000.2:n.*4T>C
ENST00000413851.2:c.*4T>C ENSP00000409000.2:n.*4T>C
ENST00000613087.4:c.*4T>C ENSP00000481633.1:n.*4T>C
XM_005258765.3:c.*4T>C XP_005258822.1:n.*4T>C
XM_011526757.1:c.*4T>C XP_011525059.1:n.*4T>C
NM_001346937.1:c.607T>C NP_001333866.1:n.607T>C
NM_172139.3:c.*4T>C NP_742151.2:n.*4T>C
NM_172139.4:c.*4T>C MANE Select NP_742151.2:n.*4T>C
NM_001346937.2:c.*4T>C NP_001333866.1:n.*4T>C
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